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Items: 1 to 20 of 118

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112673copy number variation1nstd102humanPathogenic GRCh37 chr2: 88,007,281-90,260,248 , GRCh38.p12 chr2: 87,707,762-90,221,382 IGKV3-20, IGKV3-7, 122 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5445447copy number variation1nstd206human GRCh38 chr2: 88,127,012-88,127,093 , GRCh37.p13 chr2: 88,426,531-88,426,612 FABP1
    nsv5436982copy number variation1nstd206human GRCh38 chr2: 85,539,948-89,142,574 , GRCh37.p13 chr2: 85,767,071-89,442,057 , IGKV2-18, 129 more genes
    nsv5380497translocation1nstd200human GRCh38 chr2: 88,125,478-88,125,478 , GRCh38 chr2: 88,124,211-88,124,211 , GRCh37.p13 chr2: 88,423,730-88,423,730 , GRCh37.p13 chr2: 88,424,997-88,424,997 FABP1
    nsv5341083translocation1nstd200human GRCh37 chr2: 88,424,997-88,424,997 , GRCh37 chr2: 88,423,730-88,423,730 , GRCh38.p12 chr2: 88,124,211-88,124,211 , GRCh38.p12 chr2: 88,125,478-88,125,478 FABP1
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4766632inversion1nstd199human GRCh37 chr2: 87,997,505-112,010,501 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 87,697,986-111,252,924 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr9: 40,649,751-63,450,622 , ADRA2B, 706 more genes
    nsv4752571inversion1nstd199human GRCh37 chr2: 87,550,795-112,295,517 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 87,323,672-111,537,940 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr9: 40,649,751-63,450,622 , ADRA2B, 723 more genes
    nsv4674077copy number variation1nstd102humanUncertain significance GRCh37 chr2: 88,403,403-89,129,064 , GRCh38.p12 chr2: 88,103,884-88,829,551 EIF2AK3, LOC101928347, 19 more genes
    nsv4595834copy number variation1nstd183human GRCh37 chr2: 87,737,295-89,320,921 , GRCh38.p12 chr2: 87,441,084-89,021,424 , FABP1, 61 more genes
    nsv4519735copy number variation1nstd166human GRCh37.p13 chr2: 88,290,999-88,611,000 , GRCh38.p12 chr2: 87,991,480-88,311,481 , RGPD2, 11 more genes
    nsv4064778copy number variation1nstd166human GRCh37.p13 chr2: 88,426,531-88,426,612 , GRCh38.p12 chr2: 88,127,012-88,127,093 FABP1
    nsv3910630copy number variation1nstd102humanPathogenic NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331 DAZAP2P1, RPL36AP16, 2991 more genes
    nsv3909593copy number variation1nstd102humanUncertain significance GRCh37 chr2: 87,602,598-91,619,262 , NCBI36 chr2: 87,456,109-90,982,989 , GRCh38 chr2: 87,375,475-90,282,666 LOC101928371, IGKV1-32, 130 more genes
    nsv3903029copy number variation1nstd102humanUncertain significance GRCh37 chr2: 87,325,301-92,072,301 , NCBI36 chr2: 87,178,812-91,436,028 , GRCh38 chr2: 87,098,178-91,884,275 SLC9B1P2, IGKV1-27, 158 more genes
    nsv3899461copy number variation1nstd102humanPathogenic GRCh38 chr2: 85,014,686-88,826,619 , GRCh37 chr2: 85,241,809-89,126,132 , NCBI36 chr2: 85,095,320-88,907,247 CD8A, RNU6-1007P, 115 more genes
    nsv3897079copy number variation1nstd102humanPathogenic GRCh38 chr2: 77,025,216-90,282,666 , NCBI36 chr2: 77,105,850-90,982,989 , GRCh37 chr2: 77,252,342-91,619,262 IGKV2D-18, RPIA, 280 more genes
    nsv3887199copy number variation1nstd102humanUncertain significance GRCh37 chr2: 88,180,842-89,126,291 , GRCh38.p12 chr2: 87,881,323-88,826,778 ANAPC1P5, LOC100419917, 28 more genes
    nsv3886532copy number variation1nstd102humanPathogenic GRCh37 chr2: 74,527,522-89,125,488 , GRCh38.p12 chr2: 74,300,395-88,825,975 RNU6-561P, VAMP5, 249 more genes
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